Esophagogastroduodenoscopy: Assess the gastric retention and the endoscopic mucosal visibility score during esophagogastroduodenoscopy
Study summary
A prospective, single-center, observational study to compare the risk of gastric retention and endoscopic mucosal visibility between the exposure group (one-week discontinuation of semaglutide before EGD) and non-exposure group (no semaglutide use before EGD)
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria
1. Subjects who have either: (i) been on long-term semaglutide therapy (≥4 weeks, any dosage) and discontinued use for one week prior to gastroscopy (with the last dose 8-14 days before the procedure), or(ii) never used semaglutide.
2. For patients with diabetes mellitus (DM), HbA1c \< 9% to ensure adequate glycemic control.
3. Age ≥ 18 years, with no restriction on sex.
4. American Society of Anesthesiologists (ASA) physical status classification I-II.
5. Fasting for at least 8 hours and no water intake for at least 4 hours before gastroscopy.
6. Undergoing painless (sedated) endoscopy.
Exclusion Criteria
1. History of hiatal hernia or any previous gastric surgery (including gastrectomy, Roux-en-Y gastric bypass, etc.).
2. Pregnancy.
3. Medically unfit for gastrointestinal endoscopy.
4. Deemed unsuitable for participation at the discretion of the investigators.
Primary outcome measure(s)
Rate of gastric retention — immediately after the esophagogastroduodenoscopy Gastric retention was defined as the presence of solid residues in the stomach or liquid retention exceeding 1.5 mL/kg
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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